US3481757A - Dry process porcelain enameling frit and method - Google Patents

Dry process porcelain enameling frit and method Download PDF

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Publication number
US3481757A
US3481757A US382959A US3481757DA US3481757A US 3481757 A US3481757 A US 3481757A US 382959 A US382959 A US 382959A US 3481757D A US3481757D A US 3481757DA US 3481757 A US3481757 A US 3481757A
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United States
Prior art keywords
frit
titania
formula
amount
dry process
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
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US382959A
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English (en)
Inventor
Harry J Van Dolah
Otto C Linhart
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Eagle Picher Co
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Eagle Picher Co
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Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01CRESISTORS
    • H01C1/00Details
    • H01C1/02Housing; Enclosing; Embedding; Filling the housing or enclosure
    • H01C1/034Housing; Enclosing; Embedding; Filling the housing or enclosure the housing or enclosure being formed as coating or mould without outer sheath
    • H01C1/036Housing; Enclosing; Embedding; Filling the housing or enclosure the housing or enclosure being formed as coating or mould without outer sheath on wound resistive element
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C4/00Compositions for glass with special properties
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C8/00Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/02Frit compositions, i.e. in a powdered or comminuted form
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C8/00Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/02Frit compositions, i.e. in a powdered or comminuted form
    • C03C8/04Frit compositions, i.e. in a powdered or comminuted form containing zinc
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C8/00Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/02Frit compositions, i.e. in a powdered or comminuted form
    • C03C8/06Frit compositions, i.e. in a powdered or comminuted form containing halogen
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C8/00Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/02Frit compositions, i.e. in a powdered or comminuted form
    • C03C8/08Frit compositions, i.e. in a powdered or comminuted form containing phosphorus
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2204/00Glasses, glazes or enamels with special properties
    • C03C2204/04Opaque glass, glaze or enamel
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2205/00Compositions applicable for the manufacture of vitreous enamels or glazes
    • C03C2205/02Compositions applicable for the manufacture of vitreous enamels or glazes for opaque enamels or glazes
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2207/00Compositions specially applicable for the manufacture of vitreous enamels

Definitions

  • the present invention relates to an improved titania opacified borosilicate frit composition particularly useful in dry process enameling.
  • One of the more convenient enameling procedures involves the application of a dry enameling frit onto a hot casting or the like so that the heat of the casting fuses the frit into a uniform film of enamel which readily bonds itself to the underlying surface when the enameled article is cooled.
  • a white color in the enamel it is common practice to incorporate either an antimony or zirconium opacifier into the composition and to apply suflicient amounts of such opacified frits to produce a coating on the order of 40 to 50 mils in thickness.
  • the use of antimony or zirconium opacifiers suffers from the further disadvantage that the resultant enamels are not particularly acid resistant nor is the color as white as would be desired.
  • titanium dioxide as an opacifier because of its extremely high index of refraction, which results in better hiding power and higher opacity.
  • titania can be handled reasonably well in a wet process of application, the conventional methods for opacifying frit with titania leave much to be desired when such compositions are used in the dry enameling process. Titania containing enamels frequently produce a mottled appearance which is highly objectionable in the finished article.
  • the color achieved in the enamel coating is not always the desired blue-white cast but more often is yellowish.
  • the reflectivity of the enamel surface is not as high as would be desired in high quality enameling.
  • the glass particles resulting from the quenching are then heated to a temperature at which nucleation of titanium commences. Nucleation occurs when a number of atoms present in a disordered state aggregate to form centers of crystallization. The size of the nuclei is generally believed to be on the order of 0.005 to 0.010 micron.
  • the temperature of nucleation is usually about 250 F. below the point where crystallization can take place.
  • the minimum temperature for heat treatment is well above the softening point for the glass, and is usually at least F. above the softening point as determined by an interferometer. The maximum temperature is believed to be about 400 F. above the interferometer softening temperature.
  • the heat treatment time employed in this type of process varies from about 1 minute to 25 minutes, and preferably does not exceed 15 minutes.
  • the particles can be ground to suitable frit size and screened. Generally, the frit size is chosen so that it passes almost entirely through a 10 mesh screen, and about 20% is retained on a 200 mesh screen.
  • the frit which results consists of particles of a glass matrix containing embedded therein minute titanium dioxide crystals, as the only crystallized material.
  • the remaining glass forming ingredients are in their usual amorphous form.
  • the frit can then be applied directly to heated metal objects maintained at temperatures ranging from about 1400 to 1800 F. and preferably at 1600 to 1700 F.
  • the frit is applied to the hot metal articles through a screen in the usual manner, and fuses to a uniform enamel having substantially improved masking power, a blue-white cast, improved reflectivity, higher gloss, and better texture.
  • An object of the present invention is to provide an improved porcelain enameling frit composition particularly useful in the dry process of application, said improved frit providing better flow characteristics than have heretofore been achieved in enamels of this type.
  • Another object of the invention is to provide a porcelain enameling frit opacified with titania, and having a higher gloss than the best titania opacified enamels heretofore produced.
  • Still another object of the invention is to provide a titania opacified frit composition with titania nuclei, and a suflicient amount of other additives which prevent a leathery type of texture from appearing in the final prodnet.
  • the amount of V 0 added is in the range from 0.02 to 2.0%
  • the amount of M00 is in the range from 0.02 to 2.0%
  • the amount of PbO is in the range from 0.01 to 1.0%.
  • the total amount of alkali oxide should be in the range from about to 30% by weight.
  • the total amount of acid formers should also be in the range from about 10 to 30%. It is important that the amount of acid former be somewhere near the amount of alkali metal oxides present, in order that devitrification of the other glass forming ingredients be prevented, and only the titania appear as minute nuclei. For this purpose, then, it is preferable that the amount of acid formers be approximately the same as the amount of alkali metal oxides present on a molar basis.
  • the other oxides present, the ZnO, A1 0 and MgO should also be controlled, so that the total amount of these three oxides is preferably in the range from about 1 to 3%.
  • zirconia can be added in substitution of part of the silica, but generally should not exceed about 5%.
  • vanadium, molybdenum, and lead compounds into the frits so that they will appear as the desired oxides.
  • the vanadium may be added as ammonium metavanadate, the ammonia volatilizing off under the conditions of melting.
  • the molybdenum can be added as sodium molybdate or ammonium molybdate, while the lead can be added in the form of lead sulfate, lead carbonate, or lead silicate.
  • Formula 2 consisted of Formula 1 modified to the extent of decreasing the silica by 0.30 part and adding that amount of V 0 Formula 3 consisted of the base composition of Formula 1 except that 0.60 parts of silica were replaced by that amount of V 0 Formula 4 replaced 0.30 part of silica with M00
  • Formula 5 was the same as Formula 1 except that 0.15 parts of silica were eliminated in favor of that amount of PhD.
  • Formula 6 replaced 0.60 parts of silica with 0.30 parts of V 0 and 0.30 parts M00 All of these frits were made up in the same manner, and applied by conventional dry process enameling techniques to heated cast iron. In all cases, the texture of the enamel was improved, ranging from a slight improvement with Formula Number 5, to marked improvements in Formulas 2, 3, 4 and 6.
  • Formula 8 we substituted 0.15 part of V 0 for a corresponding amount of silica.
  • Formula 9 we raised the V 0 of Formula 7 to 0.30 parts.
  • the silica was reduced to 38.16 parts, and the V 0 was raised to 0.45 parts.
  • the additive was 0.35 parts of M00
  • Formula 12 we employed 0.15 parts of PhD.
  • Formula 13 all three additives were used, comprising 0.20 parts V 0 0.20 parts M00 and 0.10 parts of PhD.
  • a titania opacified borosilicate frit composition for application to heated metal surfaces by dry process sio 2040 B203 7-25 P205 -5 ZnO o-s Na O 0-25 K20 0-25 F2 g 2 "no, 8-24 A1203 0-4 MgO 0-3 the titania present being'in the form of extremely minute nuclei capable of growinginto larger titania crystals under the conditions of dry process enameling, the total alkali metal oxide (Na O, K 0, and U 0) contents being in the range from 10 to 30% and the total acid former (B 0 P 0 and F contents being in the range from 10 to 30%, the amount of alkali metal oxides and acid formers being substantially the same on a molar basis, said frit also containing an oxide selected from the group consisting of V 0 M00 and PbO in an amount sufiicient to improve the texture of an enamel coating produced from said frit, but not in excess of 2% by weight.
  • the frit of claim 1 containing from 0.02 to 2.0% V 0 3.
  • the frit of claim 1 containing from 0.02 to 2.0% M003.
  • the titania present being in the form of extremely minute nuclei
  • the total alkali metal oxide (Na O, K 0, and Li O) contents being in the range from 10 to 30% and the total acid former (B 0 P 0 and F contents being in the range from 10 to 30%
  • the amount of alkali metal oxides and acid formers being substantially the same on a molar basis
  • said frit also containing an oxide selected from the group consisting of V 0 M00 and PhD in an amount sufficient to improve the texture of an enamel coating produced from said frit, but not in excess of 2% by weight, fusing said frit on said surface to produce an opaque porcelain enamel coating containing titania crystals of a size substantially larger than in said frit, and having a smoother texture than produced in an enamel coating of the same frit without the addition of said oxide from said group.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Glass Compositions (AREA)
US382959A 1964-07-15 1964-07-15 Dry process porcelain enameling frit and method Expired - Lifetime US3481757A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US38295964A 1964-07-15 1964-07-15

Publications (1)

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US3481757A true US3481757A (en) 1969-12-02

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Country Status (5)

Country Link
US (1) US3481757A (de)
BE (1) BE657913A (de)
DE (1) DE1496495A1 (de)
GB (1) GB1021998A (de)
NL (1) NL6413746A (de)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52144022A (en) * 1976-05-27 1977-12-01 Ngk Frit Kk Process for coating metal surface
JPS5441915A (en) * 1977-09-09 1979-04-03 Nippon Musical Instruments Mfg Enamel body
EP0059006A1 (de) * 1981-02-19 1982-09-01 Koninklijke Philips Electronics N.V. Drahtwiderstand
US5827789A (en) * 1995-01-28 1998-10-27 Cerdec Aktiengesellschaft Keramische Farben Lead-free glass composition and the use thereof
CN113185125A (zh) * 2021-04-13 2021-07-30 佛山市陶莹新型材料有限公司 一种复合增白环保釉料、陶瓷砖及其制备方法

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3045249A1 (de) * 1980-12-01 1982-07-01 Eisenwerke Fried. Wilh. Düker GmbH & Co, 8782 Karlstadt Verfahren zum aufbringen eines resistenten schutzemailueberzugs auf duktile gusskoerper
JPS5815043A (ja) * 1981-07-17 1983-01-28 Matsushita Electric Works Ltd 低融点ガラス組成物
EP0446477A1 (de) * 1990-03-08 1991-09-18 Miles Inc. Emailzusammensetzungen

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2514855A (en) * 1947-08-15 1950-07-11 Ferro Enamel Corp Process of color-correcting titania-bearing porcelain enamels
US2776899A (en) * 1953-01-09 1957-01-08 Foote Mineral Co Ceramic product and body and method of making the same
US2940941A (en) * 1953-05-26 1960-06-14 R daltqn
US3017279A (en) * 1961-02-13 1962-01-16 Eagle Picher Co Color stable white porcelain enamel and method of producing same
US3022186A (en) * 1958-01-11 1962-02-20 Bayer Ag Mixed phases with a rutile or polyrutile structure
US3098753A (en) * 1961-11-20 1963-07-23 Eagle Picher Co Porcelain enameling frit
US3216847A (en) * 1962-03-21 1965-11-09 Nat Lead Co Frit compositions for vitreous enamels
US3253939A (en) * 1962-02-19 1966-05-31 Laporte Titanium Ltd Titanium dioxide pigments

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2514855A (en) * 1947-08-15 1950-07-11 Ferro Enamel Corp Process of color-correcting titania-bearing porcelain enamels
US2776899A (en) * 1953-01-09 1957-01-08 Foote Mineral Co Ceramic product and body and method of making the same
US2940941A (en) * 1953-05-26 1960-06-14 R daltqn
US3022186A (en) * 1958-01-11 1962-02-20 Bayer Ag Mixed phases with a rutile or polyrutile structure
US3017279A (en) * 1961-02-13 1962-01-16 Eagle Picher Co Color stable white porcelain enamel and method of producing same
US3098753A (en) * 1961-11-20 1963-07-23 Eagle Picher Co Porcelain enameling frit
US3253939A (en) * 1962-02-19 1966-05-31 Laporte Titanium Ltd Titanium dioxide pigments
US3216847A (en) * 1962-03-21 1965-11-09 Nat Lead Co Frit compositions for vitreous enamels

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52144022A (en) * 1976-05-27 1977-12-01 Ngk Frit Kk Process for coating metal surface
JPS565312B2 (de) * 1976-05-27 1981-02-04
JPS5441915A (en) * 1977-09-09 1979-04-03 Nippon Musical Instruments Mfg Enamel body
JPS5641699B2 (de) * 1977-09-09 1981-09-30
EP0059006A1 (de) * 1981-02-19 1982-09-01 Koninklijke Philips Electronics N.V. Drahtwiderstand
US5827789A (en) * 1995-01-28 1998-10-27 Cerdec Aktiengesellschaft Keramische Farben Lead-free glass composition and the use thereof
US5939343A (en) * 1995-01-28 1999-08-17 Cerdec Aktiengesellschaft Keramische Farben Lead-free glass composition and the use thereof
US6057037A (en) * 1995-01-28 2000-05-02 Cerdec Aktiengesellschaft Keramische Farben Substrate coated with a lead-free glass composition
CN113185125A (zh) * 2021-04-13 2021-07-30 佛山市陶莹新型材料有限公司 一种复合增白环保釉料、陶瓷砖及其制备方法

Also Published As

Publication number Publication date
DE1496495A1 (de) 1969-01-16
BE657913A (de) 1965-07-05
NL6413746A (de) 1966-01-17
GB1021998A (en) 1966-03-09

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